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Journal of Lipid Research, Vol. 5, 156-162, April 1964
Laboratory of Metabolism, National Heart Institute, National Institutes of Health, Bethesda, Maryland
Incorporation of C14-labeled fatty acids into phospholipids by washed ghosts, prepared from human erythrocytes, required the addition of ATP and was markedly stimulated by MgCl2 and coenzyme A. Labeled palmitic acid from 1-C14-palmitoyl CoA was incorporated in the absence of added cofactors. The extent of incorporation of linoleic acid was greater than that of oleic, palmitic, or stearic acids. Of the radioactive fatty acid taken up into phospholipids 80-90% was found in the lecithin fraction. Degradation of the lecithin with Crotalus adamanteus venom established that the labeled fatty acid was located entirely in the ßbeta;-position. When whole blood was incubated with labeled fatty acid it was also found that most of the radioactivity incorporated into the ghost phospholipids was in the ßbeta;-position of lecithin. Rat erythrocyte ghosts incorporated C14-linoleic acid into phospholipids at about the same rate as did human erythrocyte ghosts. Sheep erythrocyte ghosts (which contain little lecithin) incorporated very little fatty acid into phospholipids, and none into lecithin.
Copyright © 1964 by Lipid Research, Inc.
Incorporation of fatty acids into phospholipids of erythrocyte membranes
Accepted on December 3, 1963
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